US2747009A - Stable voltaic cells - Google Patents
Stable voltaic cells Download PDFInfo
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- US2747009A US2747009A US405197A US40519754A US2747009A US 2747009 A US2747009 A US 2747009A US 405197 A US405197 A US 405197A US 40519754 A US40519754 A US 40519754A US 2747009 A US2747009 A US 2747009A
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- cell
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- voltaic
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- 239000011159 matrix material Substances 0.000 claims description 22
- 239000003792 electrolyte Substances 0.000 claims description 10
- 229910052751 metal Inorganic materials 0.000 description 38
- 239000002184 metal Substances 0.000 description 38
- 150000003839 salts Chemical class 0.000 description 19
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 16
- 239000000243 solution Substances 0.000 description 13
- 239000011701 zinc Substances 0.000 description 13
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- 229910052725 zinc Inorganic materials 0.000 description 11
- 239000010949 copper Substances 0.000 description 10
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 10
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- 239000004372 Polyvinyl alcohol Substances 0.000 description 9
- 229910052802 copper Inorganic materials 0.000 description 9
- 239000002798 polar solvent Substances 0.000 description 9
- 229920002451 polyvinyl alcohol Polymers 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 238000000576 coating method Methods 0.000 description 8
- 150000002739 metals Chemical class 0.000 description 8
- 229920000642 polymer Polymers 0.000 description 8
- 239000010408 film Substances 0.000 description 7
- 239000011888 foil Substances 0.000 description 7
- 150000002500 ions Chemical class 0.000 description 7
- 229910052782 aluminium Inorganic materials 0.000 description 6
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 6
- 235000011187 glycerol Nutrition 0.000 description 6
- 239000000463 material Substances 0.000 description 5
- 229920005989 resin Polymers 0.000 description 5
- 239000011347 resin Substances 0.000 description 5
- 239000011592 zinc chloride Substances 0.000 description 5
- 235000005074 zinc chloride Nutrition 0.000 description 5
- 229920002125 Sokalan® Polymers 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 4
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 4
- 238000001035 drying Methods 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000004014 plasticizer Substances 0.000 description 4
- 239000004584 polyacrylic acid Substances 0.000 description 4
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 229910000366 copper(II) sulfate Inorganic materials 0.000 description 3
- 238000011084 recovery Methods 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 2
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 2
- PTFCDOFLOPIGGS-UHFFFAOYSA-N Zinc dication Chemical compound [Zn+2] PTFCDOFLOPIGGS-UHFFFAOYSA-N 0.000 description 2
- -1 albumen Polymers 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000004020 conductor Substances 0.000 description 2
- 229910001431 copper ion Inorganic materials 0.000 description 2
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 description 2
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Inorganic materials [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 230000008961 swelling Effects 0.000 description 2
- 229910052718 tin Inorganic materials 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- LNAZSHAWQACDHT-XIYTZBAFSA-N (2r,3r,4s,5r,6s)-4,5-dimethoxy-2-(methoxymethyl)-3-[(2s,3r,4s,5r,6r)-3,4,5-trimethoxy-6-(methoxymethyl)oxan-2-yl]oxy-6-[(2r,3r,4s,5r,6r)-4,5,6-trimethoxy-2-(methoxymethyl)oxan-3-yl]oxyoxane Chemical compound CO[C@@H]1[C@@H](OC)[C@H](OC)[C@@H](COC)O[C@H]1O[C@H]1[C@H](OC)[C@@H](OC)[C@H](O[C@H]2[C@@H]([C@@H](OC)[C@H](OC)O[C@@H]2COC)OC)O[C@@H]1COC LNAZSHAWQACDHT-XIYTZBAFSA-N 0.000 description 1
- PYSRRFNXTXNWCD-UHFFFAOYSA-N 3-(2-phenylethenyl)furan-2,5-dione Chemical compound O=C1OC(=O)C(C=CC=2C=CC=CC=2)=C1 PYSRRFNXTXNWCD-UHFFFAOYSA-N 0.000 description 1
- ZFSGODDPMKJGJV-UHFFFAOYSA-N 5,5-dimethylimidazolidine-2,4-dione;formaldehyde Chemical compound O=C.CC1(C)NC(=O)NC1=O ZFSGODDPMKJGJV-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 241000978776 Senegalia senegal Species 0.000 description 1
- 229920001800 Shellac Polymers 0.000 description 1
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 229910000365 copper sulfate Inorganic materials 0.000 description 1
- 229960003280 cupric chloride Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000008151 electrolyte solution Substances 0.000 description 1
- DQJJMWZRDSGUJP-UHFFFAOYSA-N ethenoxyethene;furan-2,5-dione Chemical compound C=COC=C.O=C1OC(=O)C=C1 DQJJMWZRDSGUJP-UHFFFAOYSA-N 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- 229920002521 macromolecule Polymers 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 239000005518 polymer electrolyte Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920002717 polyvinylpyridine Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- ZLGIYFNHBLSMPS-ATJNOEHPSA-N shellac Chemical compound OCCCCCC(O)C(O)CCCCCCCC(O)=O.C1C23[C@H](C(O)=O)CCC2[C@](C)(CO)[C@@H]1C(C(O)=O)=C[C@@H]3O ZLGIYFNHBLSMPS-ATJNOEHPSA-N 0.000 description 1
- 239000004208 shellac Substances 0.000 description 1
- 229940113147 shellac Drugs 0.000 description 1
- 235000013874 shellac Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 239000011686 zinc sulphate Substances 0.000 description 1
- 235000009529 zinc sulphate Nutrition 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01M—PROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
- H01M6/00—Primary cells; Manufacture thereof
- H01M6/14—Cells with non-aqueous electrolyte
- H01M6/18—Cells with non-aqueous electrolyte with solid electrolyte
- H01M6/181—Cells with non-aqueous electrolyte with solid electrolyte with polymeric electrolytes
Definitions
- This invention relates to the production of essentially dry voltaic cells and, in particular, to the production of voltaic cells containing conductive resinous matrixes containing less than about 20 per cent and preferably less than about per cent of moisture.
- Primary voltaic cells are well-known in the art and, in general, comprise electrodes at different potentials and particularly electrodes of two dissimilar metals separated by an aqueous electrolyte solution.
- aqueous electrolyte solution aqueous electrolyte solution
- dry cell wherein the aqueous solution is soaked up into some kind of a matrix or gel and the unit is sealed.
- the so-called dry cell is advantageous over other voltaic cells in that it is convenient to handle and non-spillable.
- the so-called dry cell contains a great deal of water which would rapidly be lost if the unit were not sealed. This makes it necessary to use sealed containers and greatly increases the bulk and the Weight of the primary cells.
- the form of the cell is also usually limited to cylindrical shapes.
- the electrodes in this invention are usually metallic and preferably dissimilar, although concentration cells wherein both electrodes are composed of the same metal can be made, as described below. Any two metals having different positions in the electromotive series may be used and for high voltage preferably metals which are far removed from each other in their positions in the electromotive series. Since lightness and small volume are among the advantages of the primary cells of this invention, it is advantageous to use metals which are readily available in foil form.
- the pairs of dissimilar metals which may be used are zinc and copper, aluminum and copper, zinc and silver, aluminum and silver, zinc and lead, aluminum and lead, zinc and tin, and aluminum and tin.
- the resinous matrix used in the cell should have the following properties: (1) the ability to dissolve ionized metallic salts; (2) a structure such that ions can move through the matrix freely enough to carry a modest'c'urrent; and (3) strength and toughness suflicient to hold the .cell together in a form that can be handled.
- the electrolytic liquid should be one which is a swelling agent for the resin, and
- polar solvent which is a swelling agent for the resin.
- the proportion of polar solvent should be less than about 20 per cent and preferably less than about 10 per cent by Weight of the matrix.
- polar solvents which may be used in accordance with this invention are: water, ammonia, amines, glycols, glycerine and mixtures thereof. Water is the preferred polar solvent.
- the resin used in this invention is one which is swellable in the solvent for the electrolyte.
- a polymer electrolyte such as a polymeric carboxylic acid
- polyacrylic acid polymethacrylic acids and their salts
- styrene-maleic anhydride resins vinyl ether-maleic anhydride resins
- carboxymethyl cellulose carboxymethyl cellulose
- Polymeric materials other than polymeric carboxylic acids may also be used as matrixes and particularly other polymeric materials having polar properties.
- these other matrixes are: polyvinyl alcohol, polyvinyl pyr rolidone, polyvinyl pyridine, polyacrylamid, polyvinyl phthalimid, methyl cellulose, hydroxy methyl celluose, gelatin, albumen, gum arabic, casein, dimethyl hydantoinformaldehyde and phenol-formaldehyde.
- the term polymeric material as used herein includes naturally occurring macro molecules, not necessarily produced by polymerization. In general, any polymer containing polar groups in its structure is capable of absorbing and setting in an electrolytic liquid.
- the polar groups which may be present in the polymeric materials of this invention are: hydroxyl groups, carboxylic groups, amine groups, carbonyl groups, ether groups, sulfonyl groups and hydrophilic groups in general.
- the electrolytic liquid is ordinarily a solution of an ionizable salt, acid or base in a polar solvent, such as water. Any ionizable compound which is soluble in the polar solvent may be used. When water is the polar solvent, it is preferred to use, adjacent to each electrode, an ionizable water-soluble salt of the metal of the electrode.
- a polar solvent such as water
- an ionizable water-soluble salt of the metal of the electrode adjacent to each electrode.
- zinc electrode zinc chloride or zinc sulphate may comprise the ionizable salt
- copper electrode cupric chloride or cupric sulphate may comprise the ionizable salt.
- Alkaline cells using, for example, potassium or sodium hydroxide as the ionizable compound and acid cells, using dilute mineral acids, are also contemplated in this invention.
- the polymeric matrix may contain materials other than the polar solvent, the ionizable salt and the polymer itself.
- a plasticizer for the polymer may be included.
- the preferred plasticizers are glycerol and ethylene glycol, which, as stated above, also act as polar solvents.
- a depolarizer may be used.
- Fig. 1 represents graphically the load characteristics of a Cu/polyvinyl alcohol/Zn cell
- Fig. 2 represents graphically the voltage recovery rates of said cell
- Fig. 3 represents schematically said cell, partly in section.
- Example 1 were coated with small amounts of glycerol and heated 3 to effect plasticization.
- the coated panels were placed face-to-face and pressed at 70 C. under 500 p. s. i.
- the potential measured across the resultant cell by a vacuum tube voltmeter was,0.9 volt.
- Example 2 A water solution of CuClz, mixed with a water-alcohol solution of polyvinyl alcohol and glycerol, was spread on a sheet of metallic copper and dried. The resultant film was approximately 0.001 thick and its CuClz contration was about 1 M. A similar film, containing zinc chloride in 1 M concentration, was deposited on a sheet of metallic zinc.
- the coated metal sheets were laminated face-to-face at 70 C. under 500 p. s. i.
- the potential across this cell was 1.15 volts.
- Example 3 A concentration type cell was prepared in which both metlalic surfaces were .0015" aluminum foil. Two solutions of polyvinyl alcohol and glycerine, one containing 0.17M AlCls on a dry basis and the other 17M AlCla, were deposited on two pieces of aluminum foil and dried to yield coatings approximately 0.001" thick. The two coated pieces of foil were then. laminated faceto-face at 70 C. under 500 p. s. i. The potential across this cell was 0.15 volt.
- Example 4 A solution was prepared containing 8 parts by weight of polyvinyl alcohol, 2 parts by weight of ethylene glycol and 1 part by weight of cupric sulfate dissolved in 90 parts by weight of a 50-50 water-alcohol solution. A similar solution was prepared substituting 1 part by weight of zinc chloride for the cupric sulfate. The cupric sulfate solution was applied in 2 coats to a rectangular sheet of copper about ,5 thick. The zinc chloride solution was applied in 2 coats to a rectangular sheet of zinc about ,5 thick. The coated metal rectangles were dried and laminated at 200 F. at about 1000 p. s. i.
- the metal rectangles overlapped over an area of about 3 square and extended on opposite sides from this overlap area to provide a means for connecting conductors.
- This cell was tested to determine its load characteristics at 3 different temperatures, 32 F., 72 F. and 126 F. They were tested by measuring the voltage at no load and at loads varied by the substitution of resistors calibrated at 10 megohm's, 3.3 megohms, l megohm and 330,000 ohms. The results of this test are plotted semi-logarithmically in Figure 1.
- This cell was also tested to determine its voltage recovery rate at 32 F. and 72 F. This test test was run by draining the cell through a 330,000 ohm resistor for a period of about 10 minutes until the voltage was stable and then removing the resistor and measuring the rise in voltage at successive intervals of time. The results of this test are shown in Figure 2 of the drawings.
- Figure 3 of the drawings shows a single cell, partly in section, made up of a zinc sheet, a copper sheet, and a polymeric matrix.
- a polymeric matrix such as polyvinyl alcohol, containing an ionizable water-soluble metal salt, such as zinc chloride or copper sulfate, and less than about of moisture. It is to be understood that the drawing is schematic and that the relative thicknesses of the respective layers are not necessarily those shown in the drawing.
- a single cell of limited area such as those of the above examples, has a low current capacity but good stability and aging characteristics.
- Current capacity may be increased by increasing the area.
- a very long laminate of metal foils may be rolled in a manner similar to that used in the fabrication of paper condensers and thereby produce a light weight, small volume cell having a large area and increased current capacity.
- the voltage of the primary cells may be increased by the fabrication of a multi-cell battery.
- Alternate layers of 'dissimilar metal foils may be laminated with the conductive polymeric matrix sandwiched between them. For physical strength and for ease of connecting conductors, it is preferred that the outside electrodes be made of sheet metal rather than foil.
- the laminated cells and batteries produced in accordance with this invention have, intheir polymeric matrixes, a moisture content which is low enough to be stable, and which is consistent with toughness and dryness to the touch in the matrixes.
- the small exposed area of polymeric matrix between the metallic sheets need not be sealed for stability. If desired, however, a thin film of shellac or other protective coating may be applied.
- An essentially dry voltaic cell comprising a pair of electrodes at different potentials separated by a polymeric matrix containing ions of an electrolyte and less than about 10 per cent of moisture.
- An essentially dry voltaic cell comprising a pair of dissimilar metal electrodes separated by a polymeric matrix containing ions of an electrolyte and less than about 10 per cent of moisture.
- An essentially dry voltaic cell comprising a pair of dissimilar metal electrodes separated by a polymeric matrix containing less than about 10 per cent of moisture and having incorporated therein an ionized metal salt.
- An essentially dry voltaic cell comprising a pair of dissimilar metal electrodes separated by a polyacrylic acid matrix containingless than about 10 per cent of moisture and having incorporated therein an ionized metal salt.
- An essentially dry voltaic cell comprising a sheet of copper and a sheet of zinc separated by a polyacrylic acid matrix containing less than about 10 per cent of moisture and having incorporated therein an ionized metal salt.
- An essentially dry voltaic cell comprising a sheet of copper and a sheet of zinc separated by a polyacrylic acid matrix containing copper ions, zinc ions and chloride ions, and less than about 10 per cent of moisture.
- An essentially dry voltaic cell comprising a conductive resinous composition sandwiched between two sheets of dissimilar metals, said composition comprising a polymeric matrix, ions of an electrolyte and less than about 10 per cent of moisture.
- An essentially dry voltaic battery comprising a conductive resinous composition sandwiched between a plurality of sheets of alternating dissimilar metals, said composition comprising a polymeric matrix, ions of an electrolyte and less than about 10 per cent of moisture.
- An essentially dry voltaic cell prepared by coating sheets of two dissimilar metals with solid polymeric films, soaking each film in an aqueous solution of an ionizablc salt of the metal on which it is coated, drying each film to a moisture content of less than about 10 per cent by weight and compressing the sheets together with coated surfaces in contact to produce a laminate.
- An essentially dry voltaic battery prepared by coating a metal sheet with an aqueous solution comprising an ionizable salt of the metal of the sheet and a water soluble resinous polymer, drying said solution to produce a poylmeric film containing less than about 10 per cent of moisture by weight, coating a sheet of a dissimilar second metal with a Water solution of an ionizable salt of said second metal containing said water soluble resinous polymer, drying said solution to produce a polymeric film containing less than about 10 per cent of moisture by weight, compressing said coated metal sheets with coated surfaces in contact to produce a laminate.
- An essentially dry voltaic cell comprising a sheet of copper and a sheet of zinc separated by a polyvinyl alcohol matrix containing copper ions, zinc ions and chlo ride ions, and less than about 10 per cent of moisture.
- the dry voltaic cell of claim 9 which contains, in addition, glycerol as plasticizer.
- the dry voltaic cell of claim 9 which contains, in addition, an ethylene glycol as plasticizer.
- An essentially dry voltaic cell comprising a pair of dissimilar metal electrodes separated by a polymeric matrix containing less than about 10 per cent of moisture and comprising a polymer having polar properties and an ionizable, water-soluble metal salt.
- An essentially dry voltaic cell prepared by coating a metal sheet with a polymer having polar properties, coating a sheet of a second metal with the same polymer, soaking each of the coated metal sheets in an aqueous solution comprising an ionizable salt of the metal of the sheet to swell the coatings, drying said coating to a moisture concentration of less than about 10 per cent by weight, and compressing said coated metal sheets with coated surfaces in contact to produce a laminated cell.
- An essentially dry voltaic cell comprising a pair of similar metal electrodes separated by polymeric matrix containing less than about 10 per cent of moisture and having incorporated therein an ionized metal salt, said salt being present in said matrix in a high concentration in the vicinity of one of said electrodes and in a lower concentration in the vicinity of the other of said electrodes.
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- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
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- General Chemical & Material Sciences (AREA)
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Description
y 22, 1956 J. G. KIRKWOOD ET AL F'IG.I
LOAD CHARACTERISTICS OF Cu POLYVINYL ALCOHOL/ZnCELL VOLTS 5 Sheets-Sheet 1 MICROAMPERES lNVENTORS JOHN G.KIRKWOOD FRED W.WEST
ATTORNEYS May 22, 1956 J KIRKWOOD ET AL 2,747,009
STABLE VOLTAIC CELLS Filed Jan. 20, 1954 3 Sheets-Sheet 2 FIG.2
VOLTAGE RECOVERY RATES Cu/ POLYVINYL ALCOHOL/ Zn CELL INITIAL NO-LOAD EMF MIN UTES VOLTS INVENTORS JOHN G.KIRKWOOD FRED W.WEST BY r+ PM :t CQMQM ATTORNEYS May 22, 1956 .J. a. KlRkwooD ET AL 2,747,009
STABLE VOLTAIC CELLS Filed Jan. 20, 1954 3 Sheets-Sheet 3 POLYVINYL. ALCOHOL all".
INVENTORS JOHN G. KIRKWOOD FRED W. WEST By 211 QcJ/MN WC/QMQM/ ATTORNEYS United States PateiitO STABLE VOLTAIC CELLS John G. Kirkwood, Guilford, Conn., and Fred William West, Ridgefield, N. 1., assignors to The M. W. Kellogg Company, Jersey City, N. 1., a corporation of Delaware Application January 20, 1954, Serial No. 405,197
16 Claims. (Cl. 136-103) This invention relates to the production of essentially dry voltaic cells and, in particular, to the production of voltaic cells containing conductive resinous matrixes containing less than about 20 per cent and preferably less than about per cent of moisture.
Primary voltaic cells are well-known in the art and, in general, comprise electrodes at different potentials and particularly electrodes of two dissimilar metals separated by an aqueous electrolyte solution. Among the most use ful of the voltaic cells is the so-called dry cell, wherein the aqueous solution is soaked up into some kind of a matrix or gel and the unit is sealed.
The so-called dry cell is advantageous over other voltaic cells in that it is convenient to handle and non-spillable. The so-called dry cell, however, contains a great deal of water which would rapidly be lost if the unit were not sealed. This makes it necessary to use sealed containers and greatly increases the bulk and the Weight of the primary cells. The form of the cell is also usually limited to cylindrical shapes.
It has now been found that essentially dry voltaic cells can be made by using a conductive resinous composition containing ions of an electrolyte to separate the two electrodes and that such compositions may contain less than about 10 per cent of moisture. These resinous compositions are dry to the touch and will retain indefinitely their ability to permit ion migration. Such resinous composi tions need not be sealed since they cannot spill and they are not harmed by exposure to air.
The electrodes in this invention are usually metallic and preferably dissimilar, although concentration cells wherein both electrodes are composed of the same metal can be made, as described below. Any two metals having different positions in the electromotive series may be used and for high voltage preferably metals which are far removed from each other in their positions in the electromotive series. Since lightness and small volume are among the advantages of the primary cells of this invention, it is advantageous to use metals which are readily available in foil form. Among the pairs of dissimilar metals which may be used are zinc and copper, aluminum and copper, zinc and silver, aluminum and silver, zinc and lead, aluminum and lead, zinc and tin, and aluminum and tin.
If desired, however, similar electrodes may be used and the difference in potential obtained by difference in concentration and/or composition of the electrolyte in the immediate vicinity of each electrode. By the use of the resinous matrixes of this invention such difierences in the concentration and/or the composition of the electrolyte may be maintained without the use of porous diaphragms.-
The resinous matrix used in the cell should have the following properties: (1) the ability to dissolve ionized metallic salts; (2) a structure such that ions can move through the matrix freely enough to carry a modest'c'urrent; and (3) strength and toughness suflicient to hold the .cell together in a form that can be handled.
2,747,009 Patented May 22, 1956 liquid in small concentration. The electrolytic liquid should be one which is a swelling agent for the resin, and
is generally a solution of an electrolyte in a small amount of polar solvent which is a swelling agent for the resin. In order to maintain stability in the matrix, the proportion of polar solvent should be less than about 20 per cent and preferably less than about 10 per cent by Weight of the matrix. Among the polar solvents which may be used in accordance with this invention are: water, ammonia, amines, glycols, glycerine and mixtures thereof. Water is the preferred polar solvent.
The resin used in this invention is one which is swellable in the solvent for the electrolyte. Ordinarily, a polymer electrolyte such as a polymeric carboxylic acid, is used. Among the specific polymeric carboxylic acids and salts which may be used are: polyacrylic acid, polymethacrylic acids and their salts, styrene-maleic anhydride resins, vinyl ether-maleic anhydride resins, and carboxymethyl cellulose.
Polymeric materials other than polymeric carboxylic acids may also be used as matrixes and particularly other polymeric materials having polar properties. Among these other matrixes are: polyvinyl alcohol, polyvinyl pyr rolidone, polyvinyl pyridine, polyacrylamid, polyvinyl phthalimid, methyl cellulose, hydroxy methyl celluose, gelatin, albumen, gum arabic, casein, dimethyl hydantoinformaldehyde and phenol-formaldehyde. It is to be noted that the term polymeric material as used herein includes naturally occurring macro molecules, not necessarily produced by polymerization. In general, any polymer containing polar groups in its structure is capable of absorbing and setting in an electrolytic liquid. Among the polar groups which may be present in the polymeric materials of this invention are: hydroxyl groups, carboxylic groups, amine groups, carbonyl groups, ether groups, sulfonyl groups and hydrophilic groups in general.
As stated above, the electrolytic liquid is ordinarily a solution of an ionizable salt, acid or base in a polar solvent, such as water. Any ionizable compound which is soluble in the polar solvent may be used. When water is the polar solvent, it is preferred to use, adjacent to each electrode, an ionizable water-soluble salt of the metal of the electrode. For example, with a zinc electrode, zinc chloride or zinc sulphate may comprise the ionizable salt; with a copper electrode, cupric chloride or cupric sulphate may comprise the ionizable salt.
Alkaline cells, using, for example, potassium or sodium hydroxide as the ionizable compound and acid cells, using dilute mineral acids, are also contemplated in this invention.
If desired, the polymeric matrix may contain materials other than the polar solvent, the ionizable salt and the polymer itself. For example, if desired, a plasticizer for the polymer may be included. The preferred plasticizers are glycerol and ethylene glycol, which, as stated above, also act as polar solvents. Also, if desired, a depolarizer may be used.
In the drawings Fig. 1 represents graphically the load characteristics of a Cu/polyvinyl alcohol/Zn cell;
Fig. 2 represents graphically the voltage recovery rates of said cell;
Fig. 3 represents schematically said cell, partly in section.
Example 1 were coated with small amounts of glycerol and heated 3 to effect plasticization. The coated panels were placed face-to-face and pressed at 70 C. under 500 p. s. i. The potential measured across the resultant cell by a vacuum tube voltmeter was,0.9 volt.
Example 2 A water solution of CuClz, mixed with a water-alcohol solution of polyvinyl alcohol and glycerol, was spread on a sheet of metallic copper and dried. The resultant film was approximately 0.001 thick and its CuClz contration was about 1 M. A similar film, containing zinc chloride in 1 M concentration, was deposited on a sheet of metallic zinc.
The coated metal sheets were laminated face-to-face at 70 C. under 500 p. s. i. The potential across this cell was 1.15 volts.
Example 3 A concentration type cell was prepared in which both metlalic surfaces were .0015" aluminum foil. Two solutions of polyvinyl alcohol and glycerine, one containing 0.17M AlCls on a dry basis and the other 17M AlCla, were deposited on two pieces of aluminum foil and dried to yield coatings approximately 0.001" thick. The two coated pieces of foil were then. laminated faceto-face at 70 C. under 500 p. s. i. The potential across this cell was 0.15 volt.
Example 4 A solution was prepared containing 8 parts by weight of polyvinyl alcohol, 2 parts by weight of ethylene glycol and 1 part by weight of cupric sulfate dissolved in 90 parts by weight of a 50-50 water-alcohol solution. A similar solution was prepared substituting 1 part by weight of zinc chloride for the cupric sulfate. The cupric sulfate solution was applied in 2 coats to a rectangular sheet of copper about ,5 thick. The zinc chloride solution was applied in 2 coats to a rectangular sheet of zinc about ,5 thick. The coated metal rectangles were dried and laminated at 200 F. at about 1000 p. s. i. The metal rectangles overlapped over an area of about 3 square and extended on opposite sides from this overlap area to provide a means for connecting conductors. This cell was tested to determine its load characteristics at 3 different temperatures, 32 F., 72 F. and 126 F. They were tested by measuring the voltage at no load and at loads varied by the substitution of resistors calibrated at 10 megohm's, 3.3 megohms, l megohm and 330,000 ohms. The results of this test are plotted semi-logarithmically in Figure 1.
This cell was also tested to determine its voltage recovery rate at 32 F. and 72 F. This test test was run by draining the cell through a 330,000 ohm resistor for a period of about 10 minutes until the voltage was stable and then removing the resistor and measuring the rise in voltage at successive intervals of time. The results of this test are shown in Figure 2 of the drawings.
Figure 3 of the drawings shows a single cell, partly in section, made up of a zinc sheet, a copper sheet, and a polymeric matrix. such as polyvinyl alcohol, containing an ionizable water-soluble metal salt, such as zinc chloride or copper sulfate, and less than about of moisture. It is to be understood that the drawing is schematic and that the relative thicknesses of the respective layers are not necessarily those shown in the drawing.
A single cell of limited area, such as those of the above examples, has a low current capacity but good stability and aging characteristics. Current capacity may be increased by increasing the area. A very long laminate of metal foils may be rolled in a manner similar to that used in the fabrication of paper condensers and thereby produce a light weight, small volume cell having a large area and increased current capacity. If desired, the voltage of the primary cells may be increased by the fabrication of a multi-cell battery. Alternate layers of 'dissimilar metal foils may be laminated with the conductive polymeric matrix sandwiched between them. For physical strength and for ease of connecting conductors, it is preferred that the outside electrodes be made of sheet metal rather than foil. In this manner, a light weight and small volume battery, of high voltage but low current capacity, may be prepared. The laminated cells and batteries produced in accordance with this invention have, intheir polymeric matrixes, a moisture content which is low enough to be stable, and which is consistent with toughness and dryness to the touch in the matrixes. The small exposed area of polymeric matrix between the metallic sheets need not be sealed for stability. If desired, however, a thin film of shellac or other protective coating may be applied.
We claim:
1. An essentially dry voltaic cell comprising a pair of electrodes at different potentials separated by a polymeric matrix containing ions of an electrolyte and less than about 10 per cent of moisture.
2. An essentially dry voltaic cell comprising a pair of dissimilar metal electrodes separated by a polymeric matrix containing ions of an electrolyte and less than about 10 per cent of moisture.
3. An essentially dry voltaic cell comprising a pair of dissimilar metal electrodes separated by a polymeric matrix containing less than about 10 per cent of moisture and having incorporated therein an ionized metal salt.
4. An essentially dry voltaic cell comprising a pair of dissimilar metal electrodes separated by a polyacrylic acid matrix containingless than about 10 per cent of moisture and having incorporated therein an ionized metal salt.
5. An essentially dry voltaic cell comprising a sheet of copper and a sheet of zinc separated by a polyacrylic acid matrix containing less than about 10 per cent of moisture and having incorporated therein an ionized metal salt.
6. An essentially dry voltaic cell comprising a sheet of copper and a sheet of zinc separated by a polyacrylic acid matrix containing copper ions, zinc ions and chloride ions, and less than about 10 per cent of moisture.
7. An essentially dry voltaic cell comprising a conductive resinous composition sandwiched between two sheets of dissimilar metals, said composition comprising a polymeric matrix, ions of an electrolyte and less than about 10 per cent of moisture.
8. An essentially dry voltaic battery comprising a conductive resinous composition sandwiched between a plurality of sheets of alternating dissimilar metals, said composition comprising a polymeric matrix, ions of an electrolyte and less than about 10 per cent of moisture.
9. An essentially dry voltaic cell prepared by coating sheets of two dissimilar metals with solid polymeric films, soaking each film in an aqueous solution of an ionizablc salt of the metal on which it is coated, drying each film to a moisture content of less than about 10 per cent by weight and compressing the sheets together with coated surfaces in contact to produce a laminate.
10. An essentially dry voltaic battery prepared by coating a metal sheet with an aqueous solution comprising an ionizable salt of the metal of the sheet and a water soluble resinous polymer, drying said solution to produce a poylmeric film containing less than about 10 per cent of moisture by weight, coating a sheet of a dissimilar second metal with a Water solution of an ionizable salt of said second metal containing said water soluble resinous polymer, drying said solution to produce a polymeric film containing less than about 10 per cent of moisture by weight, compressing said coated metal sheets with coated surfaces in contact to produce a laminate.
11. An essentially dry voltaic cell comprising a sheet of copper and a sheet of zinc separated by a polyvinyl alcohol matrix containing copper ions, zinc ions and chlo ride ions, and less than about 10 per cent of moisture.
12. The dry voltaic cell of claim 9 which contains, in addition, glycerol as plasticizer.
13. The dry voltaic cell of claim 9 which contains, in addition, an ethylene glycol as plasticizer.
14. An essentially dry voltaic cell comprising a pair of dissimilar metal electrodes separated by a polymeric matrix containing less than about 10 per cent of moisture and comprising a polymer having polar properties and an ionizable, water-soluble metal salt.
15. An essentially dry voltaic cell prepared by coating a metal sheet with a polymer having polar properties, coating a sheet of a second metal with the same polymer, soaking each of the coated metal sheets in an aqueous solution comprising an ionizable salt of the metal of the sheet to swell the coatings, drying said coating to a moisture concentration of less than about 10 per cent by weight, and compressing said coated metal sheets with coated surfaces in contact to produce a laminated cell.
16. An essentially dry voltaic cell comprising a pair of similar metal electrodes separated by polymeric matrix containing less than about 10 per cent of moisture and having incorporated therein an ionized metal salt, said salt being present in said matrix in a high concentration in the vicinity of one of said electrodes and in a lower concentration in the vicinity of the other of said electrodes.
References Cited in the file of this patent UNITED STATES PATENTS 2,607,809 Pitzer Aug. 19, 1952 2,636,851 Juda Apr. 28, 1953 2,647,938 Taylor Aug. 4, 1953 2,648,717 Ross et al Aug. 11, 1953
Claims (1)
1. AN ESSENTIALLY DRY VOLTAIC CELL COMPRISING A PAIR OF ELECTRODES AT DIFFERENT POTENTIALS SEPARATED BY A POLYMERIC MATRIX CONTAINING IONS OF AN ELECTROLYTE AND LESS THAN ABOUT 10 PER CENT OF MOISTURE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US405197A US2747009A (en) | 1954-01-20 | 1954-01-20 | Stable voltaic cells |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US405197A US2747009A (en) | 1954-01-20 | 1954-01-20 | Stable voltaic cells |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2747009A true US2747009A (en) | 1956-05-22 |
Family
ID=23602688
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US405197A Expired - Lifetime US2747009A (en) | 1954-01-20 | 1954-01-20 | Stable voltaic cells |
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| Country | Link |
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| US (1) | US2747009A (en) |
Cited By (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2844642A (en) * | 1957-01-11 | 1958-07-22 | Schwarz Meyer | Ion exchange resin battery |
| US2851510A (en) * | 1955-11-30 | 1958-09-09 | William J Pauli | Solid battery |
| US2858353A (en) * | 1954-07-06 | 1958-10-28 | Ions Exchange & Chemical Corp | Separator for alkaline batteries |
| US2895000A (en) * | 1957-10-23 | 1959-07-14 | Schwarz Meyer | Wetting agent for ion-exchange resin battery |
| US2933547A (en) * | 1955-06-29 | 1960-04-19 | Gen Electric | Solid state electric cell |
| US2968686A (en) * | 1957-07-24 | 1961-01-17 | Electric Storage Battery Co | Sealed batteries |
| US3007992A (en) * | 1958-09-23 | 1961-11-07 | Sprague Electric Co | Battery cell structure |
| US3022367A (en) * | 1958-04-23 | 1962-02-20 | Yardney International Corp | Separator for electric batteries |
| US3023261A (en) * | 1959-11-18 | 1962-02-27 | Arnold S Louis | Monolithic electrode-separator structure for electrochemical cells |
| US3092518A (en) * | 1960-03-04 | 1963-06-04 | Union Carbide Corp | Anode film layer for galvanic cells |
| US3207633A (en) * | 1962-07-18 | 1965-09-21 | Electric Storage Battery Co | Primary alkaline cell |
| US3257242A (en) * | 1962-02-01 | 1966-06-21 | Varta Ag | Primary battery cell with a pulverulent organic polyelectrolyte |
| US3258759A (en) * | 1966-06-28 | Humidity detector | ||
| US3265536A (en) * | 1962-12-11 | 1966-08-09 | American Cyanamid Co | Alkali saturated cross-linked polyvinyl alcohol membranes and fuel cell with same |
| US3819416A (en) * | 1968-05-02 | 1974-06-25 | Gen Electric | Electrochemical cell with inside layer of water-swellable polymer |
| US3926679A (en) * | 1974-01-09 | 1975-12-16 | Monsanto Co | Phenolic resin and battery separator impregnated therewith |
| US3989540A (en) * | 1973-05-18 | 1976-11-02 | Compagnie Generale D'electricite | Method for preparing electrochemical elements in thin layers |
| FR2442513A1 (en) * | 1978-11-22 | 1980-06-20 | Anvar | Electrochemical generator for electric current prodn. - using solid soln. of ionic cpd. in polymer pref. polyoxyalkylene as electrolyte |
| FR2442512A1 (en) * | 1978-11-22 | 1980-06-20 | Anvar | NEW ELASTOMERIC MATERIALS WITH ION CONDUCTION |
| EP0145231A1 (en) * | 1983-11-02 | 1985-06-19 | Scimat Limited | Electrode article |
| US4601919A (en) * | 1984-01-18 | 1986-07-22 | Toshiba Battery Co., Ltd. | Method for preparing positive electrode for non-aqueous electrolyte cell |
| EP0360508A3 (en) * | 1988-09-22 | 1991-02-06 | Yuasa Corporation | Solid polymer electrolyte |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2607809A (en) * | 1949-01-11 | 1952-08-19 | Edgar C Pitzer | Dry cell assembly |
| US2636851A (en) * | 1949-07-09 | 1953-04-28 | Ionics | Ion-exchange materials and method of making and using the same |
| US2647938A (en) * | 1949-10-22 | 1953-08-04 | Sprague Electric Co | Combined electrolytic barrier and electrolyte |
| US2648717A (en) * | 1951-06-26 | 1953-08-11 | Sprague Electric Co | Electrolytic membrane |
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1954
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Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2607809A (en) * | 1949-01-11 | 1952-08-19 | Edgar C Pitzer | Dry cell assembly |
| US2636851A (en) * | 1949-07-09 | 1953-04-28 | Ionics | Ion-exchange materials and method of making and using the same |
| US2647938A (en) * | 1949-10-22 | 1953-08-04 | Sprague Electric Co | Combined electrolytic barrier and electrolyte |
| US2648717A (en) * | 1951-06-26 | 1953-08-11 | Sprague Electric Co | Electrolytic membrane |
Cited By (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3258759A (en) * | 1966-06-28 | Humidity detector | ||
| US2858353A (en) * | 1954-07-06 | 1958-10-28 | Ions Exchange & Chemical Corp | Separator for alkaline batteries |
| US2933547A (en) * | 1955-06-29 | 1960-04-19 | Gen Electric | Solid state electric cell |
| US2851510A (en) * | 1955-11-30 | 1958-09-09 | William J Pauli | Solid battery |
| US2844642A (en) * | 1957-01-11 | 1958-07-22 | Schwarz Meyer | Ion exchange resin battery |
| US2968686A (en) * | 1957-07-24 | 1961-01-17 | Electric Storage Battery Co | Sealed batteries |
| US2895000A (en) * | 1957-10-23 | 1959-07-14 | Schwarz Meyer | Wetting agent for ion-exchange resin battery |
| US3022367A (en) * | 1958-04-23 | 1962-02-20 | Yardney International Corp | Separator for electric batteries |
| US3007992A (en) * | 1958-09-23 | 1961-11-07 | Sprague Electric Co | Battery cell structure |
| US3023261A (en) * | 1959-11-18 | 1962-02-27 | Arnold S Louis | Monolithic electrode-separator structure for electrochemical cells |
| US3092518A (en) * | 1960-03-04 | 1963-06-04 | Union Carbide Corp | Anode film layer for galvanic cells |
| US3257242A (en) * | 1962-02-01 | 1966-06-21 | Varta Ag | Primary battery cell with a pulverulent organic polyelectrolyte |
| US3207633A (en) * | 1962-07-18 | 1965-09-21 | Electric Storage Battery Co | Primary alkaline cell |
| US3265536A (en) * | 1962-12-11 | 1966-08-09 | American Cyanamid Co | Alkali saturated cross-linked polyvinyl alcohol membranes and fuel cell with same |
| US3819416A (en) * | 1968-05-02 | 1974-06-25 | Gen Electric | Electrochemical cell with inside layer of water-swellable polymer |
| US3989540A (en) * | 1973-05-18 | 1976-11-02 | Compagnie Generale D'electricite | Method for preparing electrochemical elements in thin layers |
| US3926679A (en) * | 1974-01-09 | 1975-12-16 | Monsanto Co | Phenolic resin and battery separator impregnated therewith |
| FR2442513A1 (en) * | 1978-11-22 | 1980-06-20 | Anvar | Electrochemical generator for electric current prodn. - using solid soln. of ionic cpd. in polymer pref. polyoxyalkylene as electrolyte |
| FR2442512A1 (en) * | 1978-11-22 | 1980-06-20 | Anvar | NEW ELASTOMERIC MATERIALS WITH ION CONDUCTION |
| EP0013199A1 (en) * | 1978-11-22 | 1980-07-09 | ANVAR Agence Nationale de Valorisation de la Recherche | Electrochemical current generators and materials for their construction |
| EP0145231A1 (en) * | 1983-11-02 | 1985-06-19 | Scimat Limited | Electrode article |
| US4892559A (en) * | 1983-11-02 | 1990-01-09 | Scimat Limited | Electrode article |
| US4601919A (en) * | 1984-01-18 | 1986-07-22 | Toshiba Battery Co., Ltd. | Method for preparing positive electrode for non-aqueous electrolyte cell |
| EP0360508A3 (en) * | 1988-09-22 | 1991-02-06 | Yuasa Corporation | Solid polymer electrolyte |
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